Canonical Allele Identifier: CA1327140861
Gene: ABCA12 HGNC NCBI
SNHG31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214932399A= , CM000664.2:g.214932399A= GRCh38
NC_000002.11:g.215797123A= , CM000664.1:g.215797123A= GRCh37
NC_000002.10:g.215505368A= NCBI36
NG_007074.1:g.211029T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272895.12:c.*235T= (ABCA12) MANE Select ENSP00000272895.7:n.*235T=
ENST00000272895.11:c.*235T= (ABCA12) ENSP00000272895.7:n.*235T=
NM_015657.3:c.*235T= (ABCA12) NP_056472.2:n.*235T=
NM_173076.2:c.*235T= (ABCA12) NP_775099.2:n.*235T=
NR_103740.1:n.8323T= (ABCA12)
NR_110292.1:n.322-15426A= (SNHG31)
XM_011510951.1:c.*235T= (ABCA12) XP_011509253.1:n.*235T=
XM_011510951.2:c.*235T= (ABCA12) XP_011509253.1:n.*235T=
NM_173076.3:c.*235T= (ABCA12) MANE Select NP_775099.2:n.*235T=
NR_103740.2:n.8521T= (ABCA12)
NM_015657.4:c.*235T= (ABCA12) NP_056472.2:n.*235T=
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